Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 10

1.

Molecular and cellular effects of Tamm-Horsfall protein mutations and their rescue by chemical chaperones.

Ma L, Liu Y, El-Achkar TM, Wu XR.

J Biol Chem. 2012 Jan 6;287(2):1290-305. doi: 10.1074/jbc.M111.283036. Epub 2011 Nov 22.

3.

Protein transport into the human ER and related diseases, Sec61-channelopathies.

Haßdenteufel S, Klein MC, Melnyk A, Zimmermann R.

Biochem Cell Biol. 2014 Dec;92(6):499-509. doi: 10.1139/bcb-2014-0043. Epub 2014 May 27. Review.

PMID:
24934166
4.

F508del-CFTR rescue: a matter of cell stress response.

Nieddu E, Pollarolo B, Merello L, Schenone S, Mazzei M.

Curr Pharm Des. 2013;19(19):3476-96. Review.

PMID:
23331026
5.

Uromodulin: old friend with new roles in health and disease.

Iorember FM, Vehaskari VM.

Pediatr Nephrol. 2014 Jul;29(7):1151-8. doi: 10.1007/s00467-013-2563-z. Epub 2013 Jul 24. Review.

PMID:
23880785
6.

Uromodulin and chronic kidney disease.

Lhotta K.

Kidney Blood Press Res. 2010;33(5):393-8. doi: 10.1159/000320681. Epub 2010 Oct 14. Review.

7.

The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease.

Rampoldi L, Scolari F, Amoroso A, Ghiggeri G, Devuyst O.

Kidney Int. 2011 Aug;80(4):338-47. doi: 10.1038/ki.2011.134. Epub 2011 Jun 8. Review.

8.

Pharmacological chaperones: a new twist on receptor folding.

Morello JP, Petäjä-Repo UE, Bichet DG, Bouvier M.

Trends Pharmacol Sci. 2000 Dec;21(12):466-9. Review.

PMID:
11121835
9.

Oxidative protein folding in the endoplasmic reticulum: tight links to the mitochondria-associated membrane (MAM).

Simmen T, Lynes EM, Gesson K, Thomas G.

Biochim Biophys Acta. 2010 Aug;1798(8):1465-73. doi: 10.1016/j.bbamem.2010.04.009. Epub 2010 Apr 27. Review.

10.

Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations.

Bateman JF, Boot-Handford RP, Lamandé SR.

Nat Rev Genet. 2009 Mar;10(3):173-83. doi: 10.1038/nrg2520. Review.

PMID:
19204719

Supplemental Content

Support Center